# Isolated ventricular septal defect is not a risk factor for celiac disease: evidence from a large real-world data cohort of 493,382 children

**Authors:** Ramon Cohen, Haitham Abu Khadija, Shay Nemet, Mohammad Masu'd, Duha Najajra, Alena Kirzhner, Tal Schiller, Nizar Abu Hamdeh, Shira Bezalel-Rosenberg, Ilan Asher, Ali Abdallah, Keren Mahlab-Guri, Mohammad Alnees, Daniel Elbirt

PMC · DOI: 10.3389/fped.2026.1751030 · Frontiers in Pediatrics · 2026-03-18

## TL;DR

A large study found that isolated heart defects in children are not linked to a higher risk of celiac disease, unlike other conditions like diabetes and autoimmune diseases.

## Contribution

This study provides real-world evidence that isolated VSD is not independently associated with celiac disease in children.

## Key findings

- Isolated VSD was not independently linked to celiac disease (HR 1.25, 97.5% CI 0.85–1.82).
- Type 1 diabetes, chromosomal anomalies, and autoimmune diseases were strongly associated with celiac disease.
- The findings suggest no need for routine celiac screening based solely on VSD.

## Abstract

Ventricular septal defect (VSD) is one of the most common congenital heart defects in children. Celiac disease (CD) is known to cluster with autoimmune conditions and chromosomal syndromes, but it remains unclear whether isolated VSD is independently associated with CD.

We performed a population-based retrospective cohort study using electronic records from Clalit Health Services. Children aged 0–10 years were followed for up to 10 years to identify incident cases of CD. Multivariable Cox proportional hazards models were used to estimate adjusted hazard ratios (HRs) with 97.5% confidence intervals (CIs) for the association between VSD and CD. The models were adjusted for age, sex, type 1 diabetes mellitus, autoimmune diseases, immunodeficiency, and chromosomal anomalies.

The Cox model included 493,382 children. VSD was not independently associated with an increased risk of CD (HR 1.25, 97.5% CI 0.85–1.82). In contrast, established comorbidities showed strong associations with CD: type 1 diabetes mellitus (HR 10.26, 97.5% CI 8.15–12.91), chromosomal anomalies (HR 5.20, 97.5% CI 3.67–7.37), and autoimmune diseases (HR 2.07, 97.5% CI 1.39–3.10).

In this large real-world data, isolated VSD was not an independent risk factor for CD, whereas type 1 diabetes mellitus, chromosomal anomalies, and other autoimmune diseases were strongly associated with CD. These findings do not support routine CD screening based solely on the presence of VSD in children.

## Linked entities

- **Diseases:** celiac disease (MONDO:0005130), ventricular septal defect (MONDO:0002070), type 1 diabetes mellitus (MONDO:0005147), immunodeficiency (MONDO:0021094)

## Full-text entities

- **Diseases:** chromosomal syndromes (MESH:D025063), chromosomal anomalies (MESH:D002869), autoimmune conditions (MESH:D001327), VSD (MESH:D006345), congenital heart defects (MESH:D006330), CD (MESH:D002446), immunodeficiency (MESH:D007153), type 1 diabetes mellitus (MESH:D003922)

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038903/full.md

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Source: https://tomesphere.com/paper/PMC13038903